[1]ÂÞºìÇå,µË½à,ÐìÀö,µÈ.¶ÅÖÙË®ÌáÈ¡Îïͨ¹ýPI3K/AKT;¾¶µ÷½ÚÌú´úл¸ÄÉÆÌÇÄò²¡ÐÔ¹ÇÖÊÊèËÉ֢ʵÑéÑо¿[J].ÉÂÎ÷ҽѧÔÓÖ¾,2025,54(12):1608-1615.[doi:DOI:10.3969/j.issn.1000-7377.2025.12.004]
¡¡LUO Hongqing,DENG Jie,XU Li,et al.Eucommia ulmoides water extract regulates iron metabolism through PI3K/AKT pathway to improve diabetic osteoporosis[J].,2025,54(12):1608-1615.[doi:DOI:10.3969/j.issn.1000-7377.2025.12.004]
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54
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1608-1615
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2025-12-05

ÎÄÕÂÐÅÏ¢/Info

Title:
Eucommia ulmoides water extract regulates iron metabolism through PI3K/AKT pathway to improve diabetic osteoporosis
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Author(s):
LUO Hongqing1DENG Jie2XU Li3LU Jing1LI Honghui1KUANG Tao1LIU Caiqun1
(1.The Second Department of Spine,the First Affiliated Hospital of Hunan University of Traditional Chinese Medicine,Changsha 410007,China;2.Department of Obstetrics and Gynecology,Changsha Maternal and Child Health Hospital,Changsha 410007,China;3.The First Department of Spine,the First Affiliated Hospital of Hunan University of Traditional Chinese Medicine,Changsha 410007,China)
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Keywords:
Diabetic osteoporosisEucommia ulmoides water extractPhosphatidylinositol 3-kinaseProtein kinase BSignaling pathwayIron metabolismBone regeneration
·ÖÀàºÅ:
R 285.5
DOI:
DOI:10.3969/j.issn.1000-7377.2025.12.004
ÎÄÏ×±êÖ¾Âë:
A
ÕªÒª:
Ä¿µÄ£ºÌ½ÌÖ¶ÅÖÙ£¨EUL£©Ë®ÌáÈ¡Îïͨ¹ýÁ×Ö¬õ£¼¡´¼3-¼¤Ã¸£¨PI3K£©/µ°°×¼¤Ã¸B£¨AKT£©Í¨Â·µ÷½ÚÌú´úл¶ÔÌÇÄò²¡ÐÔ¹ÇÖÊÊèËÉÖ¢£¨DOP£©ÖеĸÄÉÆ×÷Ó᣷½·¨£º½«60Ö»SD´óÊóËæ»ú·ÖΪ¶ÔÕÕ×é¡¢DOP×éºÍEUL×飬ÿ×é20Ö»¡£Í¨¹ý¸ßÖ¬·¾Òûʳ½áºÏÁ´ëå×ô¾úËØ×¢É佨Á¢DOP´óÊóÄ£ÐÍ¡£EUL×é´óÊó¿Ú·þEULË®ÌáÈ¡Îï2.5 g/£¨kg¡¤d£©£¬¶ÔÕÕ×éºÍDOP×é¿Ú·þµÈÁ¿ÕôÁóË®£¬³ÖÐø12ÖÜ¡£Ê¹ÓÃÏÔ΢CTÆÀ¹À¹ÇÃܶȣ¨BMD£©¡¢¹ÇСÁºÊýÁ¿£¨Tb.N£©ºÍ¹ÇСÁºÌå»ý·ÖÊý£¨BV/TV£©¡£¼ì²âѪÇåÌúÀë×Ӻͱû¶þÈ©£¨MDA£©Ë®Æ½£¬²¢Í¨¹ýWestern blot·ÖÎöPI3K/AKTÐźÅͨ·Ïà¹Øµ°°×µÄ±í´ï¡£Ê¹ÓÃMC3T3-E1³É¹Çϸ°ûÄ£ÐÍ·ÖÎöEULË®ÌáÈ¡Îï¶Ôϸ°ûÔöÖ³¡¢³É¹Ç·Ö»¯¼°Ìú´úлµÄÓ°Ïì¡£½á¹û£ºÓë¶ÔÕÕ×é±È½Ï£¬DOP×é´óÊóBMD¡¢Tb.NºÍBV/TVÏÔÖø½µµÍ£¬EUL×é´óÊóBMD¡¢Tb.NºÍBV/TV½ÏDOP×éÏÔÖøÔö¼Ó£¨¾ùP<0.05£©¡£EUL´¦ÀíÏÔÖø½µµÍÁËDOP´óÊóѪÇåÌúÀë×ÓºÍMDAˮƽ£¬Í¬Ê±Ìá¸ßÁ˹Ç×éÖ¯ÖÐÁ×ËữPI3K£¨p-PI3K£©ºÍÁ×ËữAKT£¨p-AKT£©µ°°×µÄ±í´ï£¨¾ùP<0.05£©¡£ÔÚMC3T3-E1ϸ°ûÖУ¬EULÏÔÖøÌá¸ßÁ˸ßÌÇÌõ¼þϵÄϸ°ûÔöÖ³ÄÜÁ¦¡¢ALP»îÐԺ͸ƳÁ»ý£¬²¢¸ÄÉÆÁËϸ°ûµÄÌú´úлÎÉÂÒ¡£¼ÓÈëPI3KÒÖÖÆ¼ÁLY294002ºó£¬EULµÄ¸ÄÉÆÐ§¹ûÊܵ½ÒÖÖÆ¡£½áÂÛ£ºEULË®ÌáÈ¡Îïͨ¹ý¼¤»îPI3K/AKTÐźÅͨ·£¬¿ÉÓÐЧ¸ÄÉÆDOPÄ£ÐÍÖеÄÌú´úлÎÉÂҺͳɹǹ¦ÄÜÕϰ­¡£
Abstract:
Objective:To investigate the effect of Eucommia ulmoides (EUL) water extract on the improvement of diabetic osteoporosis (DOP) through regulating iron metabolism via the phosphatidylinositol 3-kinase (PI3K)/protein kinase B (AKT) pathway.Methods£ºSixty SD rats were randomly divided into the control group,the DOP group and the EUL group,with 20 rats in each group.The DOP rat model was established by using a high-fat diet combined with streptozotocin injection.The EUL group rats were orally administered 2.5 g/(kgÿ?‚¦bd) of EUL water extract,while the control group and the DOP group were orally administered the same amount of distilled water,for a duration of 12 weeks.Micro-CT was used to evaluate bone mineral density (BMD),trabecular number (Tb.N) and trabecular volume/total volume (BV/TV).Serum iron ions and malondialdehyde (MDA) levels were detected,and the expression of proteins related to the PI3K/AKT signaling pathway was analyzed by Western blot.The MC3T3-E1 osteoblast cell model was used to analyze the effects of EUL water extract on cell proliferation,osteogenic differentiation and iron metabolism.Results:Compared with the control group,the BMD,Tb.N and BV/TV in the DOP group were significantly decreased,while those in the EUL group were significantly increased compared with the DOP group (all P<0.05).EUL treatment significantly reduced the serum iron ions and MDA levels in DOP rats,and simultaneously increased the expression of p-PI3K and p-AKT proteins in bone tissue (all P<0.05).In MC3T3-E1 cells,EUL significantly enhanced the cell proliferation ability,ALP activity and calcium deposition under high glucose conditions,and improved the iron metabolism disorder of the cells.The improvement effect of EUL was inhibited after adding the PI3K inhibitor LY294002.Conclusion:The EUL water extract can effectively alleviate iron metabolism disorders and osteogenic dysfunction in the DOP model by activating the PI3K/AKT signaling pathway.

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